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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533762Generated: October 29, 2026

Acetic Anhydride → HCID 46843680, compound

https://huagongshe.com/reaction/533762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 46843679HCID 46843679—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 46843680HCID 4684368044.6%

Reaction Steps

Benzo[1,3]dioxol-5-yl-(6,7,8,9-tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrol-4-yl)-amine (50 mg, 0.16 mmol), acetic anhydride (18 μL, 0.19 mmol), and triethylamine (67 μL, 0.49 mmol) were dissolved in 1,2-dichloroethane (2 mL), and stirred overnight at room temperature. The reaction mixture was added directly to a Biotage column. The crude product was purified via Biotage eluting with a gradient of 0 to 10% MeOH in DCM. Lyophilization of the purified product provided 56 (25 mg, 44% yield) as a tan powder. LC-MS (M+H=351, obsd.=351).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853391B2
Source datasetuspto-grants-2014_10
ORD IDord-1acf6e0f309342a99ec7c4e0f0fa4ab7
Source noteuspto-grants-2014_10